Interleukin‐1 Blockade Inhibits the Acute Inflammatory Response in Patients With ST‐Segment–Elevation Myocardial Infarction

Блокада интерлейкина-1 подавляет острый воспалительный ответ у пациентов с инфарктом миокарда с подъёмом сегмента ST
Antonio Abbate, Cory R. Trankle, Leo F. Buckley, Michael J. Lipinski, Darryn Appleton, Dinesh Kadariya, Justin M. Canada, Salvatore Carbone, Charlotte S. Roberts, Nayef Abouzaki, Ryan Melchior, Sanah Christopher, Jeremy Turlington, George Mueller, James P. Garnett, Christopher S. Thomas, Roshanak Markley, George F. Wohlford, Laura Puckett, Horacio Medina de Chazal, Juan Guido Chiabrando, Edoardo Bressi, Marco Giuseppe Del Buono, Aaron Schatz, Chau Vo, Dave L. Dixon, Giuseppe Biondi‐Zoccai, Michael C. Kontos, Benjamín W. Van Tassell
2020-03-03

ST-segment elevation myocardial infarctionanakinraheart failurehigh-sensitivity C-reactive proteininterleukin-1 blockade
Background ST ‐segment–elevation myocardial infarction is associated with an intense acute inflammatory response and risk of heart failure. We tested whether interleukin‐1 blockade with anakinra significantly reduced the area under the curve for hsCRP (high sensitivity C‐reactive protein) levels during the first 14 days in patients with ST ‐segment–elevation myocardial infarction (VCUART3 [Virginia Commonwealth University Anakinra Remodeling Trial 3]). Methods and Results We conducted a randomized, placebo‐controlled, double‐blind, clinical trial in 99 patients with ST ‐segment–elevation myocardial infarction in which patients were assigned to 2 weeks treatment with anakinra once daily (N=33), anakinra twice daily (N=31), or placebo (N=35). hsCRP area under the curve was significantly lower in patients receiving anakinra versus placebo (median, 67 [interquartile range, 39–120] versus 214 [interquartile range, 131–394] mg·day/L; P <0.001), without significant differences between the anakinra arms. No significant differences were found between anakinra and placebo groups in the interval changes in left ventricular end‐systolic volume (median, 1.4 [interquartile range, −9.8 to 9.8] versus −3.9 [interquartile range, −15.4 to 1.4] mL; P =0.21) or left ventricular ejection fraction (median, 3.9% [interquartile range, −1.6% to 10.2%] versus 2.7% [interquartile range, −1.8% to 9.3%]; P =0.61) at 12 months. The incidence of death or new‐onset heart failure or of death and hospitalization for heart failure was significantly lower with anakinra versus placebo (9.4% versus 25.7% [ P =0.046] and 0% versus 11.4% [ P =0.011], respectively), without difference between the anakinra arms. The incidence of serious infection was not different between anakinra and placebo groups (14% versus 14%; P =0.98). Injection site reactions occurred more frequently in patients receiving anakinra (22%) versus placebo (3%; P =0.016). Conclusions In patients presenting with ST ‐segment–elevation myocardial infarction, interleukin‐1 blockade with anakinra significantly reduces the systemic inflammatory response compared with placebo. Clinical Trial Registration URL : https://www.clinicaltrials.gov/ . Unique identifier: NCT 01950299.
1
Anakinra did not significantly improve 12-month changes in left ventricular end-systolic volume or ejection fraction compared with placebo.
2
Anakinra reduced the incidence of death or new-onset heart failure and death or heart-failure hospitalization versus placebo.
3
Once-daily and twice-daily anakinra produced no significant difference in hsCRP area under the curve.
4
Serious infection rates were similar between groups, while injection-site reactions were more frequent with anakinra.
5
Two weeks of interleukin-1 blockade with anakinra significantly reduced the 14-day hsCRP inflammatory burden versus placebo in patients with ST-segment–elevation myocardial infarction.

Patients with ST-segment–elevation myocardial infarction treated with anakinra or placebo

The effect of interleukin-1 blockade on the acute inflammatory response, cardiac remodeling, heart-failure outcomes, and safety

Publication Details
Publication Date
2020-03-03
Journal
Publisher
ISSN
Access Type
Author Information
Authors
Antonio Abbate
Cory R. Trankle
Leo F. Buckley
Michael J. Lipinski
Darryn Appleton
Dinesh Kadariya
Justin M. Canada
Salvatore Carbone
Charlotte S. Roberts
Nayef Abouzaki
Ryan Melchior
Sanah Christopher
Jeremy Turlington
George Mueller
James P. Garnett
Christopher S. Thomas
Roshanak Markley
George F. Wohlford
Laura Puckett
Horacio Medina de Chazal
Juan Guido Chiabrando
Edoardo Bressi
Marco Giuseppe Del Buono
Aaron Schatz
Chau Vo
Dave L. Dixon
Giuseppe Biondi‐Zoccai
Michael C. Kontos
Benjamín W. Van Tassell
Explore further
Open the scid.ai AI chat with a ready-made request: it will find papers on a similar topic and help build a literature review.
Find similar papers in the chat
Make a presentation
100%